TwinLoop Flex Guide, 12° RM

FDA UDI

Class I (US FDA UDI)

by T.a.g Medical Products Agricultural Cooperative Association

Identity

Trade Name: TwinLoop Flex Guide, 12° RM FDA UDI
Generic Name: Arthroscopic obturator FDA UDI
Model / Reference: B FDA UDI

Identifiers

Catalog Number: 400104st FDA UDI
Primary DI / UDI-DI: 10810190015428 FDA UDI
FDA Product Code: LXH FDA UDI
GMDN Term: Arthroscopic obturator FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 888.4540 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Arthroscopic obturator

TwinLoop Flex Guide, 12° RM by T.a.g Medical Products Agricultural Cooperative Association — Class I — FDA UDI — listed in FDA GUDID

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: T.a.g Medical Products Agricultural Cooperative Association

Sources (1)

FDA UDI 4911e03e-1801-40af-ad01-328163ffd1ee 33 fields · synced May 30, 2026